Faten Moassas

发表

A compound heterozygous −29 A>G and IVS-I-1 G>A mutation of HBB gene leading to β-thalassemia intermedia in a Syrian patient: A case report

Hossam Murad, W. Al-achkar, Faten Moassas, 2019, Cogent Medicine.

Mutation spectrum of phenylketonuria in Syrian population: genotype-phenotype correlation.

Diana Alasmar, Hossam Murad, W. Al-achkar, 2013, Gene.

First Report on the Coinheritance of α-Thalassemia and a Rare β-Thalassemia Compound Heterozygosity for the IVS-I-I(G>A)/IVS-II-705(T>G) Mutations in a Syrian Family

Hossam Murad, Faten Moassas, 2019, Hemoglobin.

Haplotype Analysis of Three Common β-Thalassemia Mutations in Syrian Patients

Yasser Mukhalalaty, Hossam Murad, I. Ghoury, 2018, Hemoglobin.

Prenatal Molecular Diagnosis of β-Thalassemia and Sickle Cell Anemia in the Syrian Population

Yasser Mukhalalaty, R. Jarjour, Hossam Murad, 2014, Hemoglobin.

Description of a Rare β-Globin Gene Mutation: –86 (C>G) (HBB: c.-136C>G) Observed in a Syrian Family

Hossam Murad, Faten Moassas, Ayman Alabloog, 2018, Hemoglobin.

Compound heterozygosity for Hb C/Hb S (HBB: c.19G>A/HBB: c.20A>T) diseases observed in a Syrian family: a case report

Hossam Murad, Faten Moassas, Amir Daboul, 2023, Annals of medicine and surgery.

Hb Knossos (HBB: c.82G > T), β-globin CD 5 (−CT) (HBB: c.17_18delCT) and δ-globin CD 59 (−a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia

Hossam Murad, Faten Moassas, M. S. Nweder, 2019, BMC Pediatrics.

A rare gene variation cap +1 (A>C) (HBB: c. −50A>C) associated with codon 5 (‐CT) (HBB: c.17_18delCT) mutation in Syrian family

Hossam Murad, Faten Moassas, Nour A L Fakseh, 2021, Molecular genetics & genomic medicine.